Impact of residual and therapeutic doses of ciprofloxacin in the human-flora-associated mice model

被引:43
作者
Perrin-Guyomard, A
Poul, JM
Corpet, DE
Sanders, P
Fernández, AH
Bartholomew, M
机构
[1] Agence Francaise Secur Sanitaire Aliments, Lab Etud & Rech Medicaments Vet & Desinfectants, F-35302 Fougeres, France
[2] INRA, Ecole Natl Vet, Lab Secur Aliments, F-31076 Toulouse, France
[3] US FDA, Ctr Vet Med, Rockville, MD 20855 USA
关键词
human-flora-associated mouse model; intestinal flora; ciprofloxacin; veterinary drug residues;
D O I
10.1016/j.yrtph.2005.03.001
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 [法学]; 10 [医学];
摘要
A study was conducted to evaluate the effects of therapeutic and residual doses of ciprofloxacin on the human intestinal flora implanted into germ-free mice. Ciprofloxacin was administered daily via drinking water at concentrations to provide doses of 0, 0.125, 1.25, and 12.5 mg/kg b.w. Changes in the intestinal flora composition, alteration in bacterial enzyme activities, fecal short chain fatty acid concentration and bacterial cellular fatty acid profiles, overgrowth of resistant bacteria, and disruption of the colonization barrier were the endpoints evaluated in the feces of human-flora-associated (HFA) mice. Ciprofloxacin at all tested doses decreased significantly the aerobic populations and particularly the population of Enterobacteriaceae. Selection of resistant Bacteroides fragilis group was noticed in HFA mice receiving 12.5 mg/kg b.w. In mice challenged with a Salmonella strain, exogenous Salmonella persisted in the feces of all treated mice indicating that the flora responsible for the colonization barrier effect was disturbed by the antibiotic treatment. None of the studied metabolic parameters of the flora were affected by ciprofloxacin at any dose level. Under the experimental conditions of the study, the no-observed-effect level of ciprofloxacin was found to be less than 0.125 mg/kg b.w. Published by Elsevier Inc.
引用
收藏
页码:151 / 160
页数:10
相关论文
共 32 条
[1]
[Anonymous], HUMAN INTESTINAL MIC
[2]
BARRIER EFFECT OF NORMAL MICROBIOTA AGAINST CLOSTRIDIUM-DIFFICILE MAY BE INFLUENCED BY DRUGS DEVOID OF ANTIBIOTIC-ACTIVITY [J].
BARC, MC ;
DEPITRE, C ;
CORTHIER, G ;
KARJALAINEN, T ;
BOURLIOUX, P .
MICROBIAL ECOLOGY IN HEALTH AND DISEASE, 1994, 7 (06) :307-313
[3]
AN ELECTIVE AND SELECTIVE ISOLATION MEDIUM FOR BIFIDOBACTERIUM SPP [J].
BEERENS, H .
LETTERS IN APPLIED MICROBIOLOGY, 1990, 11 (03) :155-157
[4]
PHARMACOKINETICS OF CIPROFLOXACIN AND EFFECT OF REPEATED DOSAGE ON SALIVARY AND FECAL MICROFLORA [J].
BERGAN, T ;
DELIN, C ;
JOHANSEN, S ;
KOLSTAD, IM ;
NORD, CE ;
THORSTEINSSON, SB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (02) :298-302
[5]
CHANGES IN THE PHARMACOKINETICS OF CIPROFLOXACIN AND FECAL FLORA DURING ADMINISTRATION OF A 7-DAY COURSE TO HUMAN VOLUNTEERS [J].
BRUMFITT, W ;
FRANKLIN, I ;
GRADY, D ;
HAMILTONMILLER, JMT ;
ILIFFE, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (05) :757-761
[6]
CARMAN RJ, 1993, VET HUM TOXICOL, V35, P11
[7]
CORPET D, 1980, ANN INST PASTEUR MIC, VB131, P309
[9]
*CVM, 2001, DRAFT GUID ASS EFF A
[10]
DUBOS R, 1965, MAN ADAPTING, P110